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Snx9em1.1Smoc
Endonuclease-mediated Allele Detail
Summary
Symbol: Snx9em1.1Smoc
Name: sorting nexin 9; endonuclease-mediated mutation 1.1, Shanghai Model Organisms Center
MGI ID: MGI:6829641
Synonyms: Snx9deltaEx5
Gene: Snx9  Location: Chr17:5891604-5982229 bp, + strand  Genetic Position: Chr17, 3.51 cM, cytoband A1
Alliance: Snx9em1.1Smoc page
Mutation
origin
Strain of Origin:  C57BL/6
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsCRISPR-targeting introduced a loxP site upstream of exon 5 and a neomycin resistance cassette with a 3' loxP site downstream of exon 5. Cre-mediated recombination removed exon 5 and the selection cassette. (J:314970)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Snx9 Mutation:  35 strains or lines available
References
Original:  J:314970 Liu C, et al., Sorting nexin 9 (SNX9) is not essential for development and auditory function in mice. Oncotarget. 2016 Oct 18;7(42):68921-68932
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory